A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17497954



Internal ID22555888
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:8950328..8969108hg38UCSC Ensembl
chr4:8952054..8970834hg19UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg3818781
hg1918781
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5840432
Supporting Variants
Samples
Known GenesLOC650293
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17497954
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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